Zhongshan Li - Publications

Genome-wide gene expression analysis suggests an important regulatory role of lncRNAs in primary Sjögren's syndrome.

Journal: Frontiers in immunology

Published: November 21, 2025

Multi-omics integration reveals gut microbiota dysbiosis and metabolic alterations of cerebrospinal fluid in children with epilepsy.

Journal: Frontiers in microbiology

Published: May 16, 2025

Non-invasive diagnosis of primary Sjögren's syndrome using ultrasonography and transcriptome biomarkers.

Journal: Clinical immunology (Orlando, Fla.)

Published: May 06, 2023

Metagenomic Analysis Reveals A Possible Association Between Respiratory Infection and Periodontitis.

Journal: Genomics, proteomics & bioinformatics

Published: June 15, 2020

Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: December 04, 2019

Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 02, 2019

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 30, 2019

Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability.

Journal: Nature genetics

Published: March 13, 2019

Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development.

Journal: Frontiers in genetics

Published: May 31, 2018

Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: May 15, 2018

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.

Journal: American journal of human genetics

Published: August 23, 2017

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

Journal: Genome medicine

Published: August 02, 2017